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Acceptability, Usability and Preliminary Effectiveness of ChatGPT in Increasing Seasonal Influenza Vaccination Uptake Among Older Adults in Hong Kong

Acceptability, Usability and Preliminary Effectiveness of ChatGPT in Increasing Seasonal Influenza Vaccination Uptake Among Older Adults in Hong Kong

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06679647
Enrollment
50
Registered
2024-11-07
Start date
2024-12-01
Completion date
2025-03-31
Last updated
2024-11-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Behavior Change Interventions

Brief summary

In this project, we will train a ChatGPT to provide real-time answers to questions related to the SIV for older adults in Hong Kong. This study aims to evaluate the usability, acceptability, and preliminary effectiveness of the ChatGPT among 50 community-living people aged 65 years and above in Hong Kong. The primary objectives are to evaluate the usability and acceptability (including the extent of usage and subjective experiences of behavioural, cognitive, and affective engagement) of the ChatGPT at the end of the 4-week intervention period (T1). The secondary objectives are to evaluate the following conditions measured at T1, as compared to those measured at baseline (T0): 1. Self-reported uptake of SIV in the past month. 2. Changes in behavioural intention to receive SIV for the approaching flu season. 3. Changes in knowledge and attitudes related to SIV.

Interventions

BEHAVIORALAccess to a trained ChatGPT

Participants will be invited to use a trained ChatGPT which answers questions related to seasonal influenza vaccination. The functions can be used repeatedly throughout the intervention period (4 weeks), and participants will be free to spend as much time as they want on such functions.

Sponsors

Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Aged ≥65 years; * Possession of a Hong Kong ID; * Able to speak and comprehend Cantonese; * Have a smartphone with internet access; * Have not taken SIV for the approaching flu season.

Exclusion criteria

* With diagnosis of cognitive impairment or dementia; * Either blindness or deafness; * With known contraindications to the SIV as indicated by the Hong Kong Centre for Health Protection

Design outcomes

Primary

MeasureTime frameDescription
Perceived usability1 monthPerceived usability assessed by the validated Chinese version of the 10-item Perceived Usability Scale (SUS)
Extent of usage documented by the ChatGPT1 monthExtent of usage documented by the ChatGPT
Subjective experiences related to behavioural, cognitive, and affective engagement1 monthSubjective experiences related to behavioural, cognitive, and affective engagement measured by the validated Twente Engagement with eHealth Technologies Scale (TWEETS)

Contacts

Primary ContactZixin Wang, PhD
wangzx@cuhk.edu.hk+852 22528740

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026